Glenoid defect-filling component

ABSTRACT

An orthopaedic shoulder prosthesis includes glenoid defect-filling component configured to be implanted within a defect in a glenoid of a patient. The glenoid defect-filling component includes a porous metallic body and a plurality of holes formed in the porous metallic body, the plurality of holes being arranged in a pattern to receive a number of pegs of a discrete polymer glenoid component.

This application claims priority to U.S. patent application Ser. No.13/431,434, now U.S. Pat. No. 9,498,334, which was filed on Mar. 27,2012 and is expressly incorporated herein by reference.

CROSS-REFERENCE

Cross reference is made to copending U.S. patent application Ser. No.13/431,476, now U.S. Pat. No. 9,248,022, entitled “Method of Implantinga Glenoid Defect-Filing Component” by Jason Chavarria and Kyle Lappin.

TECHNICAL FIELD

The present disclosure relates generally to components and methods formodifying a glenoid surface of a scapula, and more particular, to aglenoid defect-filling component and a method of implanting the glenoiddefect-filling component within the glenoid surface of the scapula.

BACKGROUND

During the lifetime of a patient, it may be necessary to perform a totalshoulder replacement procedure on the patient as a result of, forexample, disease or trauma. In a total shoulder replacement procedure, ahumeral component having a head is utilized to replace the natural headof the arm bone or humerus. The humeral component typically has anelongated intramedullary stem that is utilized to secure the humeralcomponent to the patient's humerus. In such a total shoulder replacementprocedure, the natural glenoid surface of the scapula is resurfaced orotherwise replaced with a glenoid component which provides a bearingsurface for the head of the humeral component.

Glenoid components generally include a body that defines a bearingsurface for receiving the head of the humeral component and a number ofattachment pegs integrally formed with the body. The attachment pegs areinserted and thereafter secured into a corresponding number of holesthat are drilled in the glenoid surface of the scapula by use of bonecement.

Occasionally, the glenoid surface of the scapula includes central and/orcombined defects of the glenoid surface that provide a surface to whichit is difficult to attach a glenoid component or that are difficult totreat surgically. Current methods of treating central and/or combineddefects of the glenoid surface include bone grafting, two stage surgery,or immobilization of the joint. While these methods can be effective,they require time-intensive surgeries, multiple surgeries, and/or longrecovery times.

SUMMARY

According to an illustrative embodiment, an orthopaedic shoulderprosthesis includes a glenoid defect-filling component configured to beimplanted within a defect in a glenoid of a patient. The glenoiddefect-filling component includes a porous metallic body and a pluralityof holes formed in the porous metallic body. The holes are arranged in apattern to receive a number of pegs of a discrete polymer glenoidcomponent.

A first hole is positioned in a center of the glenoid defect-fillingcomponent, the first hole being size and shaped to receive an anchor pegof the polymer glenoid component.

A second hole is positioned between the center and an edge of theglenoid defect-filling component, the second hole being sized and shapedto receive a stabilizing peg of the polymer glenoid component.

A third hole is positioned between the center and the edge of thepolymer glenoid component, the third hole being sized and shaped toreceive a second stabilizing peg of the polymer glenoid component.

A fourth hole is positioned between the center and the edge of thepolymer glenoid component, the fourth hole being sized and shaped toreceive a third stabilizing peg of the polymer glenoid component.

The porous metallic body comprises a solid metal core with a porousmetal coating thereon.

The porous metallic body comprises a porous metal core.

According to a further illustrative embodiment, an orthopaedic glenoidprosthesis for implantation into a glenoid surface of a scapulacomprises a metallic defect-filling component sized and shaped to fitand be implanted within a defect in the glenoid surface. The metallicdefect-filling component includes a plurality of holes extendingtherethrough, the plurality of holes being arranged in a hole pattern.

The prosthesis includes a polymer glenoid component, the polymer glenoidcomponent being discrete from the metallic defect-filling component. Thepolymer glenoid component includes a bearing surface configured toarticulate with a head of a humerus and an engaging surface that isopposite the bearing surface. The engaging surface comprises a pluralityof pegs arranged in a peg pattern that corresponds to the hole patternof the metallic defect-filling component.

An anchor peg is positioned in a center of the polymer glenoidcomponent.

At least one stabilizing peg is positioned in between the center and anedge of the polymer glenoid component.

The plurality of holes in the metallic defect-filling component includesan anchor hole positioned in a center of the porous metallic body, theanchor hole being sized and shaped to receive the anchor peg of thepolymer glenoid component.

The plurality of holes in the metallic defect-filling component includesat least one stabilizing hole positioned between the center and an edgeof the metallic defect-filling component, the stabilizing hole beingsized and shaped to receive the at least one stabilizing peg of thepolymer glenoid component.

The glenoid defect-filling component includes three stabilizing holesand the glenoid defect-filling component includes three stabilizing pegsconfigured to be received within the three stabilizing holes.

The metallic defect-filling component comprises a solid metal core witha porous metal coating thereon.

The metallic defect-filling component comprises a porous metal core.

A surface of the glenoid defect-filling component in contact with thepolymer glenoid component is generally planar.

A surface of the metallic defect-filling component that is in contactwith the polymer glenoid component has a size and shape that conforms toa size and shape of a surface of the polymer glenoid in contact with themetallic defect-filling component.

According to another illustrative embodiment, an orthopaedic glenoidprosthesis for implantation into a glenoid surface of a scapulacomprises a metallic defect-filling component sized and shaped to fitand be implanted within a defect in the glenoid surface. The metallicdefect-filling component includes a first hole positioned in a center ofthe metallic defect-filling component and a second hole positionedbetween the center and an edge of the metallic defect-filling component.

The prosthesis includes a polymer glenoid component secured to themetallic defect-filling component, the polymer glenoid component beingdiscrete from the metallic defect-filling component. The polymer glenoidcomponent includes a bearing surface configured to articulate with ahead of a humerus and an engaging surface that is opposite the bearingsurface. The engaging surface includes an anchor peg positioned in acenter of the polymer glenoid component and extending into the firsthole of the metallic defect-filling component so as to secure thepolymer glenoid component to the metallic defect-filling component. Astabilizing peg is positioned between the center and an edge of thepolymer glenoid component and extends into the second hole of themetallic defect-filling component to prevent rotation of the polymerglenoid component.

The metallic defect-filling component includes three holes positionedbetween the center and the edge of the metallic defect-filling componentand the polymer glenoid component includes three stabilizing pegspositioned for insertion into the three holes of the metallicdefect-filling component.

The metallic defect-filling component includes a porous metallic bodycomprising a solid metal core with a porous metal coating thereon.

The metallic defect-filling component includes a porous metallic bodycomprising a porous metal core.

A surface of the metallic defect-filling component in contact with thepolymer glenoid component is generally planar.

A surface of the metallic defect-filling component in contact with thepolymer glenoid component has a size and shape that conforms to a sizeand shape of a surface of the polymer glenoid in contact with themetallic defect-filling component.

According to another illustrative embodiment, an orthopaedic shoulderprosthesis includes a glenoid defect-filling component configured to beimplanted within a defect in a glenoid of a patient. The glenoiddefect-filling component includes a porous metallic body and a holeformed in the porous metallic body, the hole being shaped, sized, andpositioned to receive a peg of a discrete polymer glenoid component.

Other aspects and advantages of the present disclosure will becomeapparent upon consideration of the following drawings and detaileddescription, wherein similar structures have similar reference numbers.

BRIEF DESCRIPTION OF THE DRAWINGS

The detailed description particularly refers to the following figures,in which:

FIG. 1 is a perspective view of a glenoid component;

FIGS. 2 and 3 are side elevation views of the glenoid component of FIG.1;

FIG. 4 is a top perspective view of a first embodiment of a glenoiddefect-filling component;

FIG. 5 is a side elevational view of the glenoid defect-fillingcomponent of FIG. 4 attached to the glenoid component of FIG. 1;

FIG. 6 is a top perspective view of a second embodiment of a glenoiddefect-filling component;

FIG. 7 is a bottom perspective view of the glenoid defect-fillingcomponent of FIG. 6 attached to the glenoid component of FIG. 1;

FIG. 8 is a cross-sectional view of the glenoid defect-filling componentand glenoid component of FIG. 7 taken generally along the lines 8-8 ofFIG. 7;

FIG. 9 is a top perspective view of a third embodiment of a glenoiddefect-filling component;

FIG. 10 is a perspective view of a scapula with a defect disposed withina glenoid surface of the scapula;

FIG. 11 is a perspective view of the scapula of FIG. 10 with the glenoiddefect-filling component of FIG. 8 implanted within the defect;

FIG. 12 is a perspective view of the scapula of FIG. 10 with the glenoiddefect-filling component of FIG. 8 implanted within the defect and theglenoid component being installed within the glenoid defect-fillingcomponent; and

FIG. 13 is a chart depicting various types of possible defects withinthe glenoid surface of the scapula.

DETAILED DESCRIPTION OF THE DRAWINGS

While the concepts of the present disclosure are susceptible to variousmodifications and alternative forms, specific exemplary embodimentsthereof have been shown by way of example in the drawings and willherein be described in detail. It should be understood, however, thatthere is no intent to limit the concepts of the present disclosure tothe particular forms disclosed, but on the contrary, the intention is tocover all modifications, equivalents, and alternatives falling withinthe spirit and scope of the invention as defined by the appended claims.

Terms representing anatomical references, such as anterior, posterior,medial, lateral, superior, inferior, etcetera, may be used throughoutthis disclosure in reference to both the orthopaedic implants describedherein and a patient's natural anatomy. Such terms have well-understoodmeanings in both the study of anatomy and the field of orthopaedics. Useof such anatomical reference terms in the specification and claims isintended to be consistent with their well-understood meanings unlessnoted otherwise.

Referring now to FIGS. 1-3, there is shown a polymer glenoid component20. The glenoid component 20 includes a body 22 having a first generallyconvex surface 24 and a second generally concave surface 26 opposite theconvex surface 24.

The convex surface 24 of the body 22 is configured to abut or otherwisecontact a glenoid defect-filling component, as will be discussed ingreater detail hereinafter. The concave surface 26 of the body 22provides a smooth bearing surface upon which a natural or prosthetichumeral head 32 (see FIG. 12) articulates.

The glenoid component 20 also includes an anchor peg 40 and a number ofstabilizing pegs 42 secured to and extending generally orthogonal to theconvex surface 24 of the body 22. As shown in FIGS. 1-3, the anchor peg40 includes a tapered head 48 that functions as a lead-in to facilitateinsertion into a hole drilled or otherwise formed in a glenoid surface28 of a patient's scapula 30 or within a glenoid defect-fillingcomponent, as discussed in detail below. The anchor peg 40 also includesa plurality of flexible radial fins 50 extending outwardly from a topend 52 of the anchor peg 40. The fins 50 function to secure the glenoidcomponent 20 within the glenoid surface 28 or within a glenoiddefect-filling component, as discussed below.

The stabilizing pegs 42 of the glenoid component 20 are spaced betweenthe anchor peg 40 and an outer edge 54 of the body 22. While the exactplacement and number of the stabilizing pegs 42 is not crucial, thestabilizing pegs 42 prevent the body 22 of the glenoid component 20 frommoving in a plane perpendicular to the anchor peg 40 and preventrotational movement of the glenoid component 20. Generally, thestabilizing pegs 42 are shorter than the anchor peg 34. Moreover, one ormore of the stabilizing pegs 42 may be shorter than the others, althoughother configurations may be used. While the body 22, the anchor peg 40,and the stabilizing pegs 42 of the glenoid component 20 are shown asbeing integral, one or more of the anchor peg 40 or stabilizing pegs 42may be separately secured to the body 22. As one skilled in the artwould understand, any number of anchor pegs 40 or stabilizing pegs 42may be utilized, the anchor peg 40 may include any features that aid ininserting the anchor peg 42 into a hole or retaining the anchor peg 42within a hole, and/or the placement of the anchor peg(s) 40 and/orstabilizing peg(s) 42 may be modified without departing from the scopeof the present disclosure.

The glenoid component 20, which may be used with the glenoiddefect-filling components described herein, may be made of a polymericmaterial, for example, a polyethylene. One example of a suitablepolyethylene is ultrahigh molecular weight polyethylene (UHMWPE). Inaddition to polymers, the glenoid component 20 may be made from ceramic,metal, or a composite material. Examples of these materials includealumina, zirconia, and alumina/zirconia composite or composite material.

A first embodiment of a glenoid defect-filling component 60 is depictedin FIGS. 4 and 5. The glenoid defect-filling component 60 has a body 62with a medial surface 64 a that is in contact with an inner surface 66forming a defect 68 (see FIG. 10) and a lateral surface 64 b that formsan attachment or restructured surface. The body 62 further includes agenerally oval-shaped side wall 72 extending between the surfaces 64 a,64 b and forming an outer edge of the body 60. The wall 72 includesgenerally straight walls 74 a, 74 b connected by generally round walls76 a, 76 b. A primary hole 80 extends through the body 60 between thesurfaces 64 a, 64 b. A center of the primary hole 80 is generallyaligned along a longitudinal axis 82 of the body 60 and has a firstdiameter D1. The primary hole 80 is also disposed equidistant from eachof the straight walls 74 a, 74 b of the body 60 and equidistant fromeach of the round walls 76 a, 76 b of the body 60.

A number of secondary holes 86 a-86 c extend through the body 60 betweenthe surfaces 64 a, 64 b and are disposed between the primary hole 80 andthe oval-shaped wall 72 of the body 60. The secondary hole 86 a has acenter generally aligned along the longitudinal axis 82 of the body 60and spaced between the primary hole 80 and the round wall 76 a. Thecenters of the holes 84 b, 84 c are disposed between the primary hole 80and the round wall 76 b and are further spaced outwardly of the primaryhole 80 along a lateral axis 90. Each of the secondary holes 86 a-86 chas a diameter D2 that is less than the diameter D1 of the primary hole80.

The size, shape, and placement of the primary hole 80 and the secondaryholes 86 a-86 c may be varied without departing from the scope of thepresent disclosure. In particular, the size, shape, and placement of theholes 80, 86 a-86 c will be dependent upon the particular use of theglenoid defect-filling component 60 and/or, if utilized, the design andpattern of pegs of a glenoid component for use with the glenoiddefect-filling component 60.

The glenoid defect-filling component 60 may have a body 62 made of animplant-grade biocompatible metal. Examples of such metals includecobalt, including cobalt alloys such as a cobalt chrome alloy (e.g.,CoCrMo), titanium, including titanium alloys such as a Ti6Al4V alloy,and stainless steel. The metallic material may be coated with a porousstructure, for example, a coating of cobalt-chromium alloy beads, suchas a product sold by DePuy Orthopaedics Inc. under the trade markPOROCOAT®. Optionally, the external surface of the metal body 60 may beprovided with a coating of an additional or alternative material thatpromotes bony ingrowth and/or outgrowth, such as a hydroxyapatitematerial. Still further, the external surface of the metal body 60 maybe coated with a surface treatment, such as hyaluronic acid (HA), toenhance biocompatibility. Still optionally, the body 62 of the glenoiddefect-filling component 60 may be embodied as a porous metal body in amanner similar to as described below in regard to FIG. 9.

The glenoid defect-filling component 60 of FIG. 4, or any of the otherglenoid defect-filling components disclosed herein, may be utilizedalone or in combination with cancellous or cortical graft to fill adefect in a glenoid surface 28 of the scapula 30 or may be used incombination with other treatments. In one exemplary embodiment, theglenoid defect-filling component 60 may be utilized in combination withan artificial glenoid component, such as the glenoid component 20 shownand discussed in relation to FIGS. 1-3. As seen in FIG. 5, once theglenoid defect-filling component 60 has been secured within the defect68, a discrete glenoid component 20 (or any other glenoid component) maybe secured to the glenoid defect-filling component 60. In particular,the anchor peg 40 of the glenoid component 20 is inserted into theprimary hole 80 of the glenoid defect-filling component 60 and thestabilizing pegs 42 are inserted into the secondary holes 86 a-86 c. Theflexible and deformable nature of the radial fins 50 extending from theanchor peg 40 allow the fins 50 to deform upon insertion of the anchorpeg 40 into the primary hole 80, thereby creating resistance toextraction of the anchor peg 40 from the primary hole 80 once fullyinserted therein. While the anchor peg 40 prevents removal of theglenoid component 20 from the glenoid defect-filling component 60, thestabilizing pegs 42 prevent rotational movement of the glenoid component20 and movement of the glenoid component 20 in a plane perpendicular tohe anchor peg 40.

As shown in FIG. 5, the convex medial surface 24 of the glenoidcomponent 20 abuts the lateral surface 64 b of the glenoiddefect-filling component 60. In this embodiment, the lateral surface 64b of the glenoid defect-filling component 60 is shown as having aconcave curvature that fits within the convex medial surface 24 of theglenoid component 20. Optionally, and as shown in FIGS. 7 and 8, thelateral surface 64 b may alternatively be planar, in which case, centersof the convex medial surface 24 and the lateral surface 64 b may be incontact, but the remainder of such surfaces may be spaced apart.

Referring now to FIGS. 6-8, a second embodiment of a glenoiddefect-filling component 160 similar to the glenoid defect-fillingcomponent 60 is shown. Similar elements in FIGS. 6-8 will be numbered ina similar manner as in FIGS. 4 and 5. The glenoid defect-fillingcomponent 160 includes a body 162 having a generally planar medialsurface 164 a that is in contact with the inner surface 66 forming adefect 68 (see FIG. 10) and a generally planar lateral surface 164 bthat forms an attachment or restructured surface. The body 162 furtherincludes a connecting wall 172 extending between the surfaces 164 a, 164b and forming an outer edge of the body 60. The wall 172 includes planarside walls 174 a, 174 b that are angled inwardly toward one another andconnected by generally round walls 176 a, 176 b. A radius of curvatureof the round wall 176 a is less than a radius of curvature of the roundwall 176 b. The glenoid defect-filling component 160 may be made of thesame materials as disclosed with respect to the glenoid defect-fillingcomponent 60.

As depicted in FIGS. 7 and 8, a polymer glenoid component, such as theglenoid component 20 of FIGS. 1-3, may be attached to and secured withinthe glenoid defect-filling component 160, in the same manner asdiscussed with respect to the glenoid defect-filling component 60. Inparticular, when the glenoid component 20 is attached to the glenoiddefect-filling component 160, the convex medial surface 24 of theglenoid component 20 is disposed adjacent the lateral surface 164 b ofthe glenoid defect-filling component 160. Due to the planar nature ofthe lateral surface 164 b, only edges 190 of the lateral surface 164 badjacent the primary hole 80 contact the convex medial surface 24 of theglenoid component 20. The convex medial surface 24 is otherwise spacedapart from the lateral surface 164 b. In this embodiment, prior toimplantation of the glenoid defect-filling component 60 and the glenoidcomponent 20 within the scapula 30, bone cement or graft material may beplaced into the spaces between the glenoid defect-filling component 60and the glenoid component 20, thereby providing resistance to separationof the glenoid component 20 from the glenoid defect-filling component60, and thus, the scapula 30.

Referring now to FIG. 9, a further embodiment of a glenoiddefect-filling component 260 that is similar to the glenoiddefect-filling component 160 is shown. The glenoid defect-fillingcomponent 260 of FIG. 9 is essentially the same as the glenoiddefect-filling component 160 of FIGS. 6-8 except for the configurationof its metallic 162. Specifically, in lieu of a solid metal body with aporous coating disposed thereon, the glenoid defect-filling component260 of FIG. 9 has a porous metal body. As such, when the glenoiddefect-filling component 260 is implanted in a defect 68 within theglenoid surface 28 of the patient's scapula 30, bony ingrowth into theporous metal body will occur over time.

To construct such a porous body, metal particles, such as sphericalmetal particles, are mixed with particles, such as powder particles, ofa sacrificial polymer and optionally a binding agent to bind the metalparticles to one another. Such a mixture is then molded into the desiredshape of the glenoid defect-filling component 260. Once molded into thedesired shape, the sacrificial polymer is removed by water extraction.This removes the sacrificial polymer without disturbing the shape of theglenoid defect-filling component's porous metal body. The exposedportions of the porous body promote bony ingrowth or cement adhesioninto the glenoid defect-filling component 260 when it is implanted inthe manner similar to as described below. It should be appreciated thatany desirable type of material may be used as the sacrificial polymer.One type of such material is a meltable, high molecular weighthydrophilic polymer. A specific example of one such polymer ispolyethylene oxide.

It should be appreciated that the above method of constructing a porousmetal body is but one exemplary process, with numerous other knownprocesses being contemplated for use. For example, the porous metal bodycould be formed by sintering the metal particles into the shape ofglenoid defect-filling component 260.

The glenoid defect-filling components 60, 160, 260 and any variation ofglenoid defect-filling components covered by the present disclosure maybe utilized alone, with a cancellous or cortical graft, or incombination with a glenoid component, such as the glenoid componentdepicted in FIGS. 1-3. Optionally, any glenoid component may be utilizedwith the glenoid defect-filling components disclosed herein (orvariations thereof). In particular, the glenoid component and glenoiddefect-filling component need only have peg and hole patterns,respectively, that match such that the glenoid component can be securedto the glenoid defect-filling component.

A method of filling a defect 68, such as seen in FIG. 10, within aglenoid surface 28 of a scapula 30 will now be discussed in relation tothe various manners in which the glenoid defect-filling components 60,160, 260 may be utilized.

Referring to FIG. 10, the defect 68 is generally formed by the innersurface 66 and a wall 300 that forms the general shape of the defect 68.While the methods herein will be described with respect to the defect 68as seen in FIG. 10, the methods may be utilized for any number ofdifferent defects, including those shown in FIG. 13. The wall 300 may becontinuous if the defect 68 is completely contained within the glenoidsurface 28 or may be discontinuous if the defect extends to an outeredge 302 of the glenoid surface 28.

An appropriate glenoid defect-filling component for a particular defectis selected based on the shape, size, and location of the defect withinthe glenoid surface 28. The glenoid defect-filling component, forexample, the glenoid defect-filling component 60, is implanted withinthe defect 68, as seen in FIG. 11. The glenoid defect-filling component60 may be secured within the defect 68 by cement (e.g., bone cement),press-fit, interference fit, or combination thereof. Optionally, theglenoid defect-filling component may be implanted within the glenoidsurface 28 of the scapula 30 without removing any bone tissuesurrounding the defect.

After a period of time with the glenoid defect-filling component 60implanted within the defect 68, bony ingrowth will further secure theglenoid defect-filling component 60 to the bone tissue of the patient'sscapula 30, thereby preventing the glenoid defect-filling component 60from moving out of the defect 68. In one embodiment of the method, theglenoid defect-filling component 60 is not used with other treatments.In another embodiment, the glenoid defect-filling component 60 is usedin combination with a cancellous or cortical graft, which is placed overthe glenoid defect-filling component 60.

In another embodiment of the method, as depicted in FIG. 12, afterimplantation of the glenoid defect-filling component 60 within thedefect 68, a polymer glenoid component, such as the glenoid component 20of FIGS. 1-3 may be secured to the glenoid defect-filling component 60.Prior to insertion of the glenoid component 20, a drill (not shown) maybe used to create a bore 400, as shown in FIGS. 11 and 12, within thescapula 30 that extends deeper than the defect 68. Thereafter, theanchor peg 40 of the glenoid component 20 is inserted into the primaryhole 80 of the glenoid defect-filling component 60 and into the bore 400formed in the scapula 30, as shown in FIG. 12. The stabilizing pegs 42are simultaneously inserted into the secondary holes 86 a-86 c. As notedabove, the radial fins 52 on the anchor peg 40 deform upon insertion ofthe anchor peg 40 into the primary hole 80, thereby creating resistanceto extraction of the anchor peg 40 from the primary hole 80 once fullinserted therein. Optionally, the stabilizing pegs 42 may be cementedinto the holes 86 a-86 c.

While the glenoid components and the glenoid defect-filling componentsshown in the figures and described in detail include multiple pegs andmultiple holes, respectively, a glenoid component and a glenoiddefect-filling component may alternatively include a single peg and asingle hole, respectively. In such an embodiment, the hole of theglenoid defect-filling component is shaped, sized, and positioned toreceive the peg of the glenoid component. The glenoid defect-fillingcomponent with a single hole may be made and implanted in the samemanner as discussed with respect to the previous embodiments.

In a further embodiment, any of the glenoid defect-filling componentsmay be formed with one or more windows or cut-outs. For example, awindow may be formed within a side wall of a glenoid defect-fillingcomponent, extending inwardly to expose, for example, a peg of a glenoidcomponent when the glenoid component is secured to the glenoiddefect-filling component.

As will become apparent from reading the present specification, any ofthe features of any of the embodiments disclosed herein may beincorporated within any of the other embodiments without departing fromthe scope of the present disclosure.

While the disclosure has been illustrated and described in detail in thedrawings and foregoing description, such an illustration and descriptionis to be considered as exemplary and not restrictive in character, itbeing understood that only illustrative embodiments have been shown anddescribed and that all changes and modifications that come within thespirit of the disclosure are desired to be protected.

There are a plurality of advantages of the present disclosure arisingfrom the various features of the apparatus, system, and method describedherein. It will be noted that alternative embodiments of the apparatus,system, and method of the present disclosure may not include all of thefeatures described yet still benefit from at least some of theadvantages of such features. Those of ordinary skill in the art mayreadily devise their own implementations of the apparatus, system, andmethod that incorporate one or more of the features of the presentinvention and fall within the spirit and scope of the presentdisclosure.

1. An orthopaedic shoulder prosthesis, comprising: a glenoiddefect-filling component configured to be implanted within a defect in aglenoid of a patient, the glenoid defect-filling component having: (i) aporous metallic body, and (ii) a plurality of holes formed in the porousmetallic body, the plurality of holes being arranged in a pattern toreceive a number of pegs of a discrete polymer glenoid component.
 2. Theorthopaedic shoulder prosthesis of claim 1, wherein the plurality ofholes includes (i) a first hole positioned in a center of the porousmetallic body, the first hole being sized and shaped to receive ananchor peg of the polymer glenoid component and (ii) a second holepositioned between the center and an edge of the glenoid defect-fillingcomponent, the second hole being sized and shaped to receive astabilizing peg of the polymer glenoid component.
 3. The orthopaedicshoulder prosthesis of claim 3, wherein the plurality of holes furtherincludes (iii) a third hole positioned between the center and the edgeof the polymer glenoid component, the third hole being sized and shapedto receive a second stabilizing peg of the polymer glenoid component,and (iv) a fourth hole positioned between the center and the edge of thepolymer glenoid component, the fourth hole being sized and shaped toreceive a third stabilizing peg of the polymer glenoid component.
 4. Theorthopaedic shoulder prosthesis of claim 1, wherein the porous metallicbody comprises a solid metal core with a porous metal coating thereon.5. The orthopaedic shoulder prosthesis of claim 1, wherein the porousmetallic body comprises a porous metal core.
 6. An orthopaedic glenoidprosthesis for implantation into a glenoid surface of a scapula so as toprovide a bearing surface for a natural or prosthetic head of a humerus,the glenoid prosthesis comprising: a metallic defect-filling componentsized and shaped to fit and be implanted within a defect in the glenoidsurface, the metallic defect-filling component having a plurality ofholes extending therethrough, the plurality of holes being arranged in ahole pattern, and a polymer glenoid component, the polymer glenoidcomponent being discrete from the metallic defect-filling component andhaving (i) a bearing surface configured to articulate with the head ofthe humerus, and (ii) an engaging surface that is opposite the bearingsurface, the engaging surface comprising a plurality of pegs arranged ina peg pattern that corresponds to the hole pattern of the metallicdefect-filling component.
 7. The orthopaedic glenoid prosthesis of claim6, wherein the plurality of pegs in the polymer glenoid componentincludes (i) an anchor peg positioned in a center of the polymer glenoidcomponent, and (ii) at least one stabilizing peg positioned between thecenter and an edge of the polymer glenoid component.
 8. The orthopaedicglenoid prosthesis of claim 7, wherein the plurality of holes in themetallic defect-filling component includes (i) an anchor hole positionedin a center of the porous metallic body, the anchor hole being sized andshaped to receive the anchor peg of the polymer glenoid component and(ii) at least one stabilizing hole positioned between the center and anedge of the metallic defect-filling component, the stabilizing holebeing sized and shaped to receive the at least one stabilizing peg ofthe polymer glenoid component.
 9. The orthopaedic glenoid prosthesis ofclaim 8, wherein the metallic defect-filling component includes threestabilizing holes and the polymer glenoid component includes threestabilizing pegs configured to be received within the three stabilizingholes.
 10. The orthopaedic glenoid prosthesis of claim 6, wherein themetallic defect-filling component comprises a solid metal core with aporous metal coating thereon.
 11. The orthopaedic glenoid prosthesis ofclaim 6, wherein the metallic defect-filling component comprises aporous metal core.
 12. The orthopaedic glenoid prosthesis of claim 6,wherein a surface of the metallic defect-filling component in contactwith the polymer glenoid component is generally planar.
 13. Theorthopaedic glenoid prosthesis of claim 6, wherein a surface of themetallic defect-filling component that is in contact with the polymerglenoid component has a size and shape that conforms to a size and shapeof a surface of the polymer glenoid in contact with the metallicdefect-filling component.
 14. An orthopaedic glenoid prosthesis forimplantation into a glenoid surface of a scapula so as to provide abearing surface for a natural or prosthetic head of a humerus, theglenoid prosthesis comprising: a metallic defect-filling component sizedand shaped to fit and be implanted within a defect in the glenoidsurface, the metallic defect-filling component having (i) a first holepositioned in the center of the metallic defect-filling component, and(ii) a second hole positioned between the center and an edge of themetallic defect-filling component; and a polymer glenoid componentsecured to the metallic defect-filling component, the polymer glenoidcomponent being discrete from the metallic defect-filling component andhaving (i) a bearing surface configured to articulate with the head ofthe humerus, and (ii) an engaging surface that is opposite the bearingsurface, the engaging surface comprising (a) an anchor peg positioned ina center of the polymer glenoid component and extending into the firsthole of the metallic defect-filling component so as to secure thepolymer glenoid component to the metallic defect-filling component, and(ii) a stabilizing peg positioned between the center and an edge of thepolymer glenoid component and extending into the second hole of themetallic defect-filling component to prevent rotation of the polymerglenoid component.
 15. The orthopaedic glenoid prosthesis of claim 14,wherein the metallic defect-filling component includes three stabilizingholes positioned between the center and the edge of the metallicdefect-filling component and the polymer glenoid component includesthree stabilizing pegs positioned for insertion into the threestabilizing holes of the metallic defect-filling component.
 16. Theorthopaedic glenoid prosthesis of claim 14, wherein the metallicdefect-filling component includes a porous metallic body comprising asolid metal core with a porous metal coating thereon.
 17. Theorthopaedic glenoid prosthesis of claim 14, wherein the metallicdefect-filling component includes a porous metallic body comprising aporous metal core.
 18. The orthopaedic glenoid prosthesis of claim 6,wherein a surface of the metallic defect-filling component in contactwith the polymer glenoid component is generally planar.
 19. Theorthopaedic glenoid prosthesis of claim 6, wherein a surface of themetallic defect-filling component in contact with the polymer glenoidcomponent has a size and shape that conforms to a size and shape of asurface of the polymer glenoid in contact with the metallicdefect-filling component.
 20. An orthopaedic shoulder prosthesis,comprising: a glenoid defect-filling component configured to beimplanted within a defect in a glenoid of a patient, the glenoiddefect-filling component having: (i) a porous metallic body, and (ii) ahole formed in the porous metallic body, the hole being shaped, sized,and positioned to receive a peg of a discrete polymer glenoid component.